Disease: SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869320690
rs869320690
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1
CUI: C4225272
Disease:
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE 		0.800 GeneticVariation UNIPROT Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. 26026163 2015
dbSNP: rs869320690
rs869320690
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1
CUI: C4225272
Disease:
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE 		G 0.800 CausalMutation CLINVAR